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Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium

Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade...

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Autores principales: Vasquez, Sergio X., Gao, Feng, Su, Feng, Grijalva, Victor, Pope, John, Martin, Bill, Stinstra, Jeroen, Masner, Matthew, Shah, Neha, Weinstein, David M., Farias-Eisner, Robin, Reddy, Srinivasa T.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078938/
https://www.ncbi.nlm.nih.gov/pubmed/21533123
http://dx.doi.org/10.1371/journal.pone.0019099
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author Vasquez, Sergio X.
Gao, Feng
Su, Feng
Grijalva, Victor
Pope, John
Martin, Bill
Stinstra, Jeroen
Masner, Matthew
Shah, Neha
Weinstein, David M.
Farias-Eisner, Robin
Reddy, Srinivasa T.
author_facet Vasquez, Sergio X.
Gao, Feng
Su, Feng
Grijalva, Victor
Pope, John
Martin, Bill
Stinstra, Jeroen
Masner, Matthew
Shah, Neha
Weinstein, David M.
Farias-Eisner, Robin
Reddy, Srinivasa T.
author_sort Vasquez, Sergio X.
collection PubMed
description Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade relatively rapidly, diminishing within a few hours or days. Additionally, live animal specimens must not be subject to long duration scans, which can cause high levels of radiation exposure to the specimen, limiting the quality of images that can be captured. Lastly, despite technological advances in live-animal specimen imaging, it is quite difficult to minimize or prevent movement of a live animal, which can cause motion artifacts in the final data output. It is demonstrated here that through the use of postmortem perfusion protocols of radiopaque silicone polymer mediums and ex-vivo organ harvest, it is possible to acquire a high level of vascular signal in preclinical specimens through the use of micro-computed tomographic (microCT) imaging. Additionally, utilizing high-order rendering algorithms, it is possible to further derive vessel morphometrics for qualitative and quantitative analysis.
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spelling pubmed-30789382011-04-29 Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium Vasquez, Sergio X. Gao, Feng Su, Feng Grijalva, Victor Pope, John Martin, Bill Stinstra, Jeroen Masner, Matthew Shah, Neha Weinstein, David M. Farias-Eisner, Robin Reddy, Srinivasa T. PLoS One Research Article Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade relatively rapidly, diminishing within a few hours or days. Additionally, live animal specimens must not be subject to long duration scans, which can cause high levels of radiation exposure to the specimen, limiting the quality of images that can be captured. Lastly, despite technological advances in live-animal specimen imaging, it is quite difficult to minimize or prevent movement of a live animal, which can cause motion artifacts in the final data output. It is demonstrated here that through the use of postmortem perfusion protocols of radiopaque silicone polymer mediums and ex-vivo organ harvest, it is possible to acquire a high level of vascular signal in preclinical specimens through the use of micro-computed tomographic (microCT) imaging. Additionally, utilizing high-order rendering algorithms, it is possible to further derive vessel morphometrics for qualitative and quantitative analysis. Public Library of Science 2011-04-18 /pmc/articles/PMC3078938/ /pubmed/21533123 http://dx.doi.org/10.1371/journal.pone.0019099 Text en Vasquez et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Vasquez, Sergio X.
Gao, Feng
Su, Feng
Grijalva, Victor
Pope, John
Martin, Bill
Stinstra, Jeroen
Masner, Matthew
Shah, Neha
Weinstein, David M.
Farias-Eisner, Robin
Reddy, Srinivasa T.
Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
title Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
title_full Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
title_fullStr Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
title_full_unstemmed Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
title_short Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
title_sort optimization of microct imaging and blood vessel diameter quantitation of preclinical specimen vasculature with radiopaque polymer injection medium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078938/
https://www.ncbi.nlm.nih.gov/pubmed/21533123
http://dx.doi.org/10.1371/journal.pone.0019099
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